Evidence map›Paper›PMID 17276344›Full record

ArticleDevelopmental cell2007

The master switch gene sex-lethal promotes female development by negatively regulating the N-signaling pathway.

Jill K M Penn, Paul Schedl

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
0.9field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 30 citations in OpenAlex.

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  15. Sex-lethal enables germline stem cell differentiation by down-regulating Nanos protein levels during Drosophila oogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2012
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  20. Hrp48 attenuates Sxl expression to allow for proper notch expression and signaling in wing development.Proceedings of the National Academy of Sciences of the United States of America · 2010
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Jill K M PennDepartment of Molecular Biology, Princeton University, Princeton, NJ 08540, USA.
Paul Schedl
Princeton University · US

Funding

Sex Determination in DrosphiliaR01GM025976 · NIGMS · PRINCETON UNIVERSITY · PI SCHEDL, PAUL D · 1985 to 2007
$3.2M
NIGMS NIH HHS R01 GM025976
6 · The paper itself

Abstract

Notch (N) signaling is used for cell-fate determination in many different developmental contexts. Here, we show that the master control gene for sex determination in Drosophila melanogaster, Sex-lethal (Sxl), negatively regulates the N-signaling pathway in females. In genetic assays, reducing Sxl activity suppresses the phenotypic effects of N mutations, while increasing Sxl activity enhances the effects. Sxl appears to negatively regulate the pathway by reducing N protein accumulation, and higher levels of N are found in Sxl(-) clones than in adjacent wild-type cells. The inhibition of N expression does not depend on the known downstream targets of Sxl; however, we find that Sxl protein can bind to N mRNAs. Finally, our results indicate that downregulation of the N pathway by Sxl contributes to sex-specific differences in morphology and suggest that it may also play an important role in follicle cell specification during oogenesis.

Indexed as

Down-RegulationGenes, SwitchSex Determination ProcessesSignal TransductionAllelesAnimalsClone CellsDrosophila melanogasterDrosophila ProteinsFemaleMaleMutationOvarian FollicleOvumPhenotypeProtein BindingDrosophila ProteinsReceptors, NotchRNA-Binding ProteinsRNA, MessengerSxl protein, Drosophila

Identifiers

PMID17276344
PMCPMC4362774
OpenAlexW1966974824

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.